Regulations.gov document

Submission and Review of Sterility Information in Premarket Notification (510(k))…

Other · FDA-2008-D-0611 · posted Jan 8, 2024

Key facts

Document ID FDA-2008-D-0611-0018
Title Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile; Guidance for Industry and Food and Drug Administration Staff
Document type Other
Subtype Guidance
Agency FDA
Docket FDA-2008-D-0611
Posted Jan 8, 2024
Comment period opens Jan 8, 2024

At a glance

  • 10–99 Public comments on this docket

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